{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1721","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1719","results":[{"created":"2020-07-22T06:57:48.670997+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TWIST1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Robinow-Sorauf syndrome, MIM# 180750; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TWIST1","entity_type":"gene"},{"created":"2020-07-22T00:03:29.114979+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TWIST1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TWIST1","entity_type":"gene"},{"created":"2020-07-22T00:02:56.331637+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TTC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TTC8","entity_type":"gene"},{"created":"2020-07-22T00:02:27.109463+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TTC21B was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"TTC21B","entity_type":"gene"},{"created":"2020-07-22T00:01:56.853388+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRAF3IP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRAF3IP1","entity_type":"gene"},{"created":"2020-07-22T00:01:18.616741+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMEM67 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM67","entity_type":"gene"},{"created":"2020-07-22T00:00:44.387452+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMEM237 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM237","entity_type":"gene"},{"created":"2020-07-22T00:00:12.865250+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMEM231 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM231","entity_type":"gene"},{"created":"2020-07-21T23:59:40.633345+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMEM216 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM216","entity_type":"gene"},{"created":"2020-07-21T23:59:10.787994+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMEM138 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM138","entity_type":"gene"},{"created":"2020-07-21T23:58:39.052059+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TFAP2B was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TFAP2B","entity_type":"gene"},{"created":"2020-07-21T23:58:10.534130+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TFAP2A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TFAP2A","entity_type":"gene"},{"created":"2020-07-21T23:57:41.757615+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TCTN3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TCTN3","entity_type":"gene"},{"created":"2020-07-21T23:57:12.647281+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TCTN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TCTN2","entity_type":"gene"},{"created":"2020-07-21T23:56:44.231210+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TCTEX1D2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TCTEX1D2","entity_type":"gene"},{"created":"2020-07-21T23:56:15.756962+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBX5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBX5","entity_type":"gene"},{"created":"2020-07-21T23:55:39.657437+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBX3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TBX3","entity_type":"gene"},{"created":"2020-07-21T23:55:10.744888+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TBX22 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"TBX22","entity_type":"gene"},{"created":"2020-07-21T23:54:39.222196+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SPINT2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SPINT2","entity_type":"gene"},{"created":"2020-07-21T23:54:08.497896+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMOC1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMOC1","entity_type":"gene"},{"created":"2020-07-21T23:53:01.457208+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SHH was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SHH","entity_type":"gene"},{"created":"2020-07-21T23:48:15.088427+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SDCCAG8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SDCCAG8","entity_type":"gene"},{"created":"2020-07-21T23:47:39.897364+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SC5D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SC5D","entity_type":"gene"},{"created":"2020-07-21T23:47:11.435242+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SALL4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL4","entity_type":"gene"},{"created":"2020-07-21T23:46:42.317976+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SALL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL1","entity_type":"gene"},{"created":"2020-07-21T23:39:30.630447+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RPGRIP1L was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RPGRIP1L","entity_type":"gene"},{"created":"2020-07-21T23:38:49.889949+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RBM10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RBM10","entity_type":"gene"},{"created":"2020-07-21T23:38:21.248050+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAB23 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB23","entity_type":"gene"},{"created":"2020-07-21T23:37:36.640129+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PROM1 as ready","entity_name":"PROM1","entity_type":"gene"},{"created":"2020-07-21T23:37:36.632661+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prom1 has been classified as Red List (Low Evidence).","entity_name":"PROM1","entity_type":"gene"},{"created":"2020-07-21T23:37:32.108202+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PROM1 were changed from  to Cone-rod dystrophy 12, MIM# 612657; Macular dystrophy, retinal, 2, MIM# 608051; Retinitis pigmentosa 41, MIM# 612095; Stargardt disease 4, MIM# 603786","entity_name":"PROM1","entity_type":"gene"},{"created":"2020-07-21T23:37:02.675415+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PROM1 as Red List (low evidence)","entity_name":"PROM1","entity_type":"gene"},{"created":"2020-07-21T23:37:02.662440+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prom1 has been classified as Red List (Low Evidence).","entity_name":"PROM1","entity_type":"gene"},{"created":"2020-07-21T23:36:38.012393+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PROM1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Cone-rod dystrophy 12, MIM# 612657, Macular dystrophy, retinal, 2, MIM# 608051, Retinitis pigmentosa 41, MIM# 612095, Stargardt disease 4, MIM# 603786; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PROM1","entity_type":"gene"},{"created":"2020-07-21T23:33:21.824558+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PROM1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PROM1","entity_type":"gene"},{"created":"2020-07-21T23:32:50.303827+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PORCN was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"PORCN","entity_type":"gene"},{"created":"2020-07-21T23:32:17.072577+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PNPLA6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PNPLA6","entity_type":"gene"},{"created":"2020-07-21T23:31:45.509457+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PITX1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PITX1","entity_type":"gene"},{"created":"2020-07-21T23:31:05.750009+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PIK3R2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PIK3R2","entity_type":"gene"},{"created":"2020-07-21T23:30:36.833981+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIK3CA as ready","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2020-07-21T23:30:36.829388+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Germline variants also described.","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2020-07-21T23:30:36.794888+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pik3ca has been classified as Green List (High Evidence).","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2020-07-21T23:30:33.699274+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PIK3CA were changed from  to Megalencephaly-capillary malformation (MCAP) syndrome , MIM#602501","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2020-07-21T23:28:34.928018+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PIK3CA was changed from Unknown to Other","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2020-07-21T23:28:05.570306+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Tag somatic tag was added to gene: PIK3CA.","entity_name":"PIK3CA","entity_type":"gene"},{"created":"2020-07-21T23:27:41.608729+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OFD1 was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"OFD1","entity_type":"gene"},{"created":"2020-07-21T23:27:11.005675+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NPHP3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NPHP3","entity_type":"gene"},{"created":"2020-07-21T23:26:42.950564+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NEK1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NEK1","entity_type":"gene"},{"created":"2020-07-21T23:26:14.769341+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MKS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MKS1","entity_type":"gene"},{"created":"2020-07-21T23:25:46.491276+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MKKS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MKKS","entity_type":"gene"},{"created":"2020-07-21T23:25:19.214008+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MEGF8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"MEGF8","entity_type":"gene"},{"created":"2020-07-21T23:24:49.218950+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MBTPS2 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"MBTPS2","entity_type":"gene"},{"created":"2020-07-21T23:24:20.592340+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.104","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LZTFL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LZTFL1","entity_type":"gene"},{"created":"2020-07-21T23:23:36.376392+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: LRP4: Changed phenotypes: Cenani-Lenz syndactyly syndrome, MIM# 212780, Sclerosteosis 2, MIM# 614305","entity_name":"LRP4","entity_type":"gene"},{"created":"2020-07-21T23:23:26.598744+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LRP4 as ready","entity_name":"LRP4","entity_type":"gene"},{"created":"2020-07-21T23:23:26.591670+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrp4 has been classified as Red List (Low Evidence).","entity_name":"LRP4","entity_type":"gene"},{"created":"2020-07-21T23:23:16.337700+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: LRP4: Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"LRP4","entity_type":"gene"},{"created":"2020-07-21T23:23:05.387774+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LRP4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"LRP4","entity_type":"gene"},{"created":"2020-07-21T23:22:44.098169+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LRP4 as Red List (low evidence)","entity_name":"LRP4","entity_type":"gene"},{"created":"2020-07-21T23:22:44.091785+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lrp4 has been classified as Red List (Low Evidence).","entity_name":"LRP4","entity_type":"gene"},{"created":"2020-07-21T23:22:26.639877+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LRP4 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"LRP4","entity_type":"gene"},{"created":"2020-07-21T23:22:09.352168+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LRP4 were changed from  to Cenani-Lenz syndactyly syndrome, MIM#\t212780; Sclerosteosis 2, MIM#\t614305","entity_name":"LRP4","entity_type":"gene"},{"created":"2020-07-21T23:19:34.789734+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LMBR1 were changed from  to Polydactyly, preaxial type II, MIM#\t174500","entity_name":"LMBR1","entity_type":"gene"},{"created":"2020-07-21T23:19:18.152430+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LMBR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LMBR1","entity_type":"gene"},{"created":"2020-07-21T23:18:06.101992+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LBR as ready","entity_name":"LBR","entity_type":"gene"},{"created":"2020-07-21T23:18:06.091617+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lbr has been classified as Green List (High Evidence).","entity_name":"LBR","entity_type":"gene"},{"created":"2020-07-21T23:18:01.508835+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LBR were changed from  to Greenberg skeletal dysplasia, MIM#\t215140","entity_name":"LBR","entity_type":"gene"},{"created":"2020-07-21T23:17:35.469404+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LBR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LBR","entity_type":"gene"},{"created":"2020-07-21T23:16:31.635034+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIF7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KIF7","entity_type":"gene"},{"created":"2020-07-21T23:16:04.548160+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KIAA0586 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KIAA0586","entity_type":"gene"},{"created":"2020-07-21T23:15:23.745163+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: INPP5E was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"INPP5E","entity_type":"gene"},{"created":"2020-07-21T23:14:57.892770+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT80","entity_type":"gene"},{"created":"2020-07-21T23:14:23.908138+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT52 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT52","entity_type":"gene"},{"created":"2020-07-21T23:13:52.813772+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT43 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT43","entity_type":"gene"},{"created":"2020-07-21T23:13:25.931605+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT27 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT27","entity_type":"gene"},{"created":"2020-07-21T23:12:59.545305+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT172 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT172","entity_type":"gene"},{"created":"2020-07-21T23:12:32.686126+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IFT140 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IFT140","entity_type":"gene"},{"created":"2020-07-21T23:11:58.931690+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ICK was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ICK","entity_type":"gene"},{"created":"2020-07-21T23:11:18.696404+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HYLS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HYLS1","entity_type":"gene"},{"created":"2020-07-21T23:10:53.299364+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HOXD13 were changed from  to Synpolydactyly 1, MIM#\t186000","entity_name":"HOXD13","entity_type":"gene"},{"created":"2020-07-21T23:10:30.276638+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HOXD13 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HOXD13","entity_type":"gene"},{"created":"2020-07-21T23:09:44.347288+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HOXA13 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HOXA13","entity_type":"gene"},{"created":"2020-07-21T23:09:17.603614+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HNRNPK was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HNRNPK","entity_type":"gene"},{"created":"2020-07-21T23:08:47.346515+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GRIP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GRIP1","entity_type":"gene"},{"created":"2020-07-21T23:08:18.720895+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GPC3 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"GPC3","entity_type":"gene"},{"created":"2020-07-21T23:07:47.207515+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GLI3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GLI3","entity_type":"gene"},{"created":"2020-07-21T23:07:23.112115+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GLI2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"GLI2","entity_type":"gene"},{"created":"2020-07-21T23:06:53.960848+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GDF5 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"GDF5","entity_type":"gene"},{"created":"2020-07-21T23:06:25.430339+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FREM2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FREM2","entity_type":"gene"},{"created":"2020-07-21T23:05:59.815070+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FRAS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FRAS1","entity_type":"gene"},{"created":"2020-07-21T23:05:34.656089+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGFR3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR3","entity_type":"gene"},{"created":"2020-07-21T23:05:08.450304+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGFR2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR2","entity_type":"gene"},{"created":"2020-07-21T23:04:43.725203+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGFR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGFR1","entity_type":"gene"},{"created":"2020-07-21T23:04:17.242201+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FGF10 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"FGF10","entity_type":"gene"},{"created":"2020-07-21T23:03:51.040218+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EVC2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"EVC2","entity_type":"gene"},{"created":"2020-07-21T23:03:25.435790+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EVC was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"EVC","entity_type":"gene"},{"created":"2020-07-21T23:02:33.963874+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EVC was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EVC","entity_type":"gene"},{"created":"2020-07-21T23:01:46.790517+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EBP was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"EBP","entity_type":"gene"},{"created":"2020-07-21T23:01:19.687269+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DYNC2LI1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DYNC2LI1","entity_type":"gene"},{"created":"2020-07-21T23:00:55.125030+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DYNC2H1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DYNC2H1","entity_type":"gene"}]}